Reeves, P.L.S., Rudraraju, R., Wong, Florence ORCID: https://orcid.org/0000-0002-2812-8845, Hamilton-Williams, E.E. and Steptoe, R.J. 2017. Antigen presenting cell-targeted proinsulin expression converts insulin-specific CD8(+) T-cell priming to tolerance in autoimmune-prone NOD mice. European Journal of Immunology 47 (9) , pp. 1550-1561. 10.1002/eji.201747089 |
Abstract
Type 1 diabetes (T1D) results from autoimmune destruction of insulin-producing pancreatic β cells. Therapies need to incorporate strategies to overcome the genetic defects that impair induction or maintenance of peripheral T-cell tolerance and contribute to disease development. We tested whether the enforced expression of an islet autoantigen in antigen-presenting cells (APC) counteracted peripheral T-cell tolerance defects in autoimmune-prone NOD mice. We observed that insulin-specific CD8+ T cells transferred to mice in which proinsulin was transgenically expressed in APCs underwent several rounds of division and the majority were deleted. Residual insulin-specific CD8+ T cells were rendered unresponsive and this was associated with TCR downregulation, loss of tetramer binding and expression of a range of co-inhibitory molecules. Notably, accumulation and effector differentiation of insulin-specific CD8+ T cells in pancreatic lymph nodes was prominent in non-transgenic recipients but blocked by transgenic proinsulin expression. This shift from T-cell priming to T-cell tolerance exemplifies the tolerogenic capacity of autoantigen expression by APC and the capacity to overcome genetic tolerance defects. This article is protected by copyright. All rights reserved.
Item Type: | Article |
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Date Type: | Publication |
Status: | Published |
Schools: | Medicine |
Subjects: | R Medicine > R Medicine (General) |
Uncontrolled Keywords: | APC; Autoimmunity; CD8+ T cell; Gene therapy; Insulin; NOD mice; Tolerance |
Publisher: | John Wiley & Sons |
ISSN: | 0014-2980 |
Date of First Compliant Deposit: | 10 July 2017 |
Date of Acceptance: | 23 June 2017 |
Last Modified: | 02 Nov 2022 11:30 |
URI: | https://orca.cardiff.ac.uk/id/eprint/102218 |
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